A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705087



Internal ID15441739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:44552714..44556436hg38UCSC Ensembl
Innerchr6:44520451..44524173hg19UCSC Ensembl
Innerchr6:44628429..44632151hg18UCSC Ensembl
Innerchr6:44628429..44632151hg17UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg383723
hg193723
hg183723
hg173723
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528484
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705087
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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